http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1874783-B1

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filingDate 2006-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bd1eecf1f0e40eaebef55ff19d8f7e2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_134d0302d0b7f4e1efb98f7b5632c393
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df89ad17efbbbb2caf93ae1dd5fca42a
publicationDate 2010-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1874783-B1
titleOfInvention Substituted oxa-diaza-spiro-[5.5]-undecanone derivatives and their use as neurokinin antagonists
abstract This invention concerns substituted oxa-diaza-spiro-[5.5]-undecanone derivatives having neurokinin antagonistic activity, in particular an NK1 antagonistic activity, an NK3 antagonistic activity, a combined NK1/NK2 antagonistic activity and a combined NK1/NK2/NK3 antagonistic activity, their preparation, compositions comprising them and their use as a medicine, in particular for the treatment and/or prophylaxis of schizophrenia, emesis, anxiety and depression, irritable bowel syndrome (IBS), circadian rhythm disturbances, pre-eclampsia, nociception, pain, in particular visceral and neuropathic pain, pancreatitis, neurogenic inflammation, asthma, chronic obstructive pulmonary disease (COPD) and micturition disorders such as urinary incont inence. The compounds according to the invention can be represented by general Formula (I) and comprises also the pharmaceutically acceptable acid or base addition salts thereof, the stereochemically isomeric forms thereof, the N-oxide form thereof and prodrugs thereof, wherein all substituents are defined as in Claim 1.
priorityDate 2005-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 529.